ClinVar Miner

List of variants in gene LMNA reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 93
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HGVS dbSNP
NM_005572.4(LMNA):c.1242C>T (p.Ser414=) rs184946451
NM_005572.4(LMNA):c.1381-6C>T rs371635492
NM_005572.4(LMNA):c.1551G>A (p.Gln517=) rs41314035
NM_005572.4(LMNA):c.895A>G (p.Ile299Val) rs150924946
NM_170707.4(LMNA):c.1011G>C (p.Leu337=) rs753179748
NM_170707.4(LMNA):c.1029G>C (p.Arg343=) rs1553265680
NM_170707.4(LMNA):c.1051A>C (p.Arg351=) rs771623461
NM_170707.4(LMNA):c.1071C>T (p.Asp357=) rs376875762
NM_170707.4(LMNA):c.1155G>A (p.Glu385=) rs878855232
NM_170707.4(LMNA):c.1158-10C>T rs1572363723
NM_170707.4(LMNA):c.1161A>G (p.Leu387=) rs1572363770
NM_170707.4(LMNA):c.1173C>T (p.Pro391=) rs1553265807
NM_170707.4(LMNA):c.1185G>T (p.Ser395=) rs397517890
NM_170707.4(LMNA):c.1227A>G (p.Thr409=) rs762130433
NM_170707.4(LMNA):c.1261C>T (p.Leu421=) rs1194745110
NM_170707.4(LMNA):c.1299C>T (p.His433=) rs61217436
NM_170707.4(LMNA):c.12G>A (p.Pro4=) rs369823958
NM_170707.4(LMNA):c.1311C>T (p.Ser437=) rs763224059
NM_170707.4(LMNA):c.1314G>A (p.Gly438=) rs774817302
NM_170707.4(LMNA):c.1317C>A (p.Arg439=) rs374804871
NM_170707.4(LMNA):c.1317C>T (p.Arg439=) rs374804871
NM_170707.4(LMNA):c.1374C>T (p.Ser458=) rs1572364784
NM_170707.4(LMNA):c.1381-6C>G rs371635492
NM_170707.4(LMNA):c.1383C>T (p.Asp461=) rs1278554399
NM_170707.4(LMNA):c.138C>T (p.Ile46=) rs1553261914
NM_170707.4(LMNA):c.1407C>A (p.Ile469=) rs1471045711
NM_170707.4(LMNA):c.1413C>G (p.Arg471=) rs1572365626
NM_170707.4(LMNA):c.1488+7G>A rs374209100
NM_170707.4(LMNA):c.1489-9C>T rs374324602
NM_170707.4(LMNA):c.150C>T (p.Arg50=) rs397517894
NM_170707.4(LMNA):c.1530C>T (p.Thr510=) rs138098342
NM_170707.4(LMNA):c.153G>T (p.Ser51=) rs751886390
NM_170707.4(LMNA):c.15C>T (p.Ser5=) rs1572331734
NM_170707.4(LMNA):c.1605G>A (p.Gly535=) rs769398087
NM_170707.4(LMNA):c.1609-4C>T rs1553266259
NM_170707.4(LMNA):c.1609-7C>T rs1372108861
NM_170707.4(LMNA):c.1656C>T (p.Asp552=) rs370219874
NM_170707.4(LMNA):c.1680C>T (p.Asp560=) rs17847249
NM_170707.4(LMNA):c.1699-4C>T rs1394491459
NM_170707.4(LMNA):c.1699-8C>G rs727503137
NM_170707.4(LMNA):c.1699-9_1699-8del rs1572369030
NM_170707.4(LMNA):c.1701C>T (p.Gly567=) rs1174456476
NM_170707.4(LMNA):c.1731T>C (p.Ala577=) rs776066211
NM_170707.4(LMNA):c.1749G>A (p.Ser583=) rs970494454
NM_170707.4(LMNA):c.1755C>T (p.Thr585=) rs545752475
NM_170707.4(LMNA):c.1767G>C (p.Gly589=) rs1572369259
NM_170707.4(LMNA):c.1770C>T (p.Thr590=) rs397517896
NM_170707.4(LMNA):c.1773C>T (p.Cys591=) rs397517897
NM_170707.4(LMNA):c.1785C>T (p.Ala595=) rs748139390
NM_170707.4(LMNA):c.1803C>T (p.Ser601=) rs267607604
NM_170707.4(LMNA):c.1804G>A (p.Gly602Ser) rs60662302
NM_170707.4(LMNA):c.1818G>A (p.Gln606=) rs1060504514
NM_170707.4(LMNA):c.1857T>C (p.Ser619=) rs368581237
NM_170707.4(LMNA):c.1890G>A (p.Gly630=) rs770389147
NM_170707.4(LMNA):c.1899G>A (p.Gly633=) rs1572369732
NM_170707.4(LMNA):c.1912G>A (p.Gly638Arg) rs144851946
NM_170707.4(LMNA):c.192C>T (p.Thr64=) rs137969290
NM_170707.4(LMNA):c.1930C>T (p.Arg644Cys) rs142000963
NM_170707.4(LMNA):c.1931G>A (p.Arg644His) rs368386019
NM_170707.4(LMNA):c.1941C>T (p.Leu647=) rs984562109
NM_170707.4(LMNA):c.1969-4T>C rs751715969
NM_170707.4(LMNA):c.1978A>G (p.Asn660Asp) rs374926367
NM_170707.4(LMNA):c.339T>C (p.Phe113=) rs759878335
NM_170707.4(LMNA):c.346C>T (p.Leu116=) rs876657491
NM_170707.4(LMNA):c.372G>A (p.Glu124=) rs1572352924
NM_170707.4(LMNA):c.471G>A (p.Thr157=) rs150645079
NM_170707.4(LMNA):c.477G>A (p.Glu159=) rs1424758064
NM_170707.4(LMNA):c.496C>A (p.Arg166=) rs370200334
NM_170707.4(LMNA):c.513+8C>T rs1060504515
NM_170707.4(LMNA):c.643C>T (p.Leu215=) rs397517905
NM_170707.4(LMNA):c.681G>A (p.Val227=) rs769896881
NM_170707.4(LMNA):c.711T>C (p.Phe237=) rs768081358
NM_170707.4(LMNA):c.726G>A (p.Ala242=) rs763625309
NM_170707.4(LMNA):c.74G>T (p.Arg25Leu) rs61578124
NM_170707.4(LMNA):c.771G>A (p.Glu257=) rs1471649557
NM_170707.4(LMNA):c.789G>A (p.Leu263=) rs148557956
NM_170707.4(LMNA):c.78C>T (p.Ile26=) rs373721390
NM_170707.4(LMNA):c.822C>G (p.Ala274=) rs1572360747
NM_170707.4(LMNA):c.852G>A (p.Leu284=) rs1273837882
NM_170707.4(LMNA):c.870G>A (p.Glu290=) rs747275587
NM_170707.4(LMNA):c.885G>A (p.Ser295=) rs776999079
NM_170707.4(LMNA):c.897C>T (p.Ile299=) rs762718963
NM_170707.4(LMNA):c.909T>A (p.Ser303=) rs1432653704
NM_170707.4(LMNA):c.927C>A (p.Leu309=) rs752558753
NM_170707.4(LMNA):c.936+7C>T rs757401091
NM_170707.4(LMNA):c.937-5T>C rs1001248677
NM_170707.4(LMNA):c.937-6C>T rs759083379
NM_170707.4(LMNA):c.937-8C>A rs751707982
NM_170707.4(LMNA):c.937-9C>T rs1332011298
NM_170707.4(LMNA):c.93G>A (p.Glu31=) rs878855235
NM_170707.4(LMNA):c.951G>A (p.Glu317=) rs1278448557
NM_170707.4(LMNA):c.96G>A (p.Lys32=) rs775429079
NM_170707.4(LMNA):c.990G>A (p.Glu330=) rs140800215

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